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关于谷氨酰胺结合蛋白K(GlnK)和谷氨酰胺结合蛋白B(GlnB)在调节肺炎克雷伯菌NifL依赖性氮控制中的作用的研究。

Studies on the roles of GlnK and GlnB in regulating Klebsiella pneumoniae NifL-dependent nitrogen control.

作者信息

Arcondéguy T, van Heeswijk W C, Merrick M

机构信息

Department of Molecular Microbiology, John Innes Centre, Norwich, UK.

出版信息

FEMS Microbiol Lett. 1999 Nov 15;180(2):263-70. doi: 10.1111/j.1574-6968.1999.tb08805.x.

Abstract

In Klebsiella pneumoniae, nitrogen fixation (nif) genes are regulated in response to fixed nitrogen and oxygen. The activity of the nif-specific transcriptional activator NifA is modulated by NifL, which mediates both oxygen and nitrogen control. The signal transduction protein GlnK is required to relieve the inhibitory effect of NifL on NifA that occurs when the intracellular N status is high and in a wild-type cell, the action of GlnK cannot be substituted by the structurally related protein PII. We have studied the modulation of NifA activity by NifL in an heterologous system in which the host organism is Escherichia coli. Using a DeltaglnB, DeltaglnK mutant, we have shown that the modulation of NifA activity by NifL is dependent on the concentration of GlnK in the cell and that when overproduced, PII can substitute for GlnK. Furthermore, our data suggest that PII can counteract the positive action of GlnK in relieving NifL-dependent inhibition of NifA activity. This negative effect of PII may be physiologically important in establishing repression of nif gene expression when the intracellular nitrogen status rises.

摘要

在肺炎克雷伯菌中,固氮(nif)基因的表达受固定态氮和氧气的调控。nif特异性转录激活因子NifA的活性受NifL的调节,NifL介导氧气和氮的控制。信号转导蛋白GlnK是解除NifL对NifA抑制作用所必需的,这种抑制作用在细胞内氮含量高时发生,并且在野生型细胞中,GlnK的作用不能被结构相关蛋白PII替代。我们在以大肠杆菌为宿主的异源系统中研究了NifL对NifA活性的调节。使用DeltaglnB、DeltaglnK突变体,我们发现NifL对NifA活性的调节依赖于细胞内GlnK的浓度,并且当PII过量表达时,可以替代GlnK。此外,我们的数据表明PII可以抵消GlnK在解除NifL对NifA活性抑制方面的正向作用。当细胞内氮含量升高时,PII的这种负向作用在建立对nif基因表达的抑制方面可能具有重要的生理意义。

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